Functional imaging using fluorescent indicators has revolutionized biology, but additional sensor scaffolds are needed to access properties such as bright, far-red emission. Here, we introduce a new platform for 'chemigenetic' fluorescent indicators, utilizing the self-labeling HaloTag protein conjugated to environmentally sensitive synthetic fluorophores. We solve a crystal structure of HaloTag bound to a rhodamine dye ligand to guide engineering efforts to modulate the dye environment. We show that fusion of HaloTag with protein sensor domains that undergo conformational changes near the bound dye results in large and rapid changes in fluorescence output. This generalizable approach affords bright, far-red calcium and voltage sensors with highly tunable photophysical and chemical properties, which can reliably detect single action potentials in cultured neurons.
Representative scheme of Haloalkane_dehalogenase-HLD2 structure and an image from PDBsum server
Databases
PDB-Sum
6U2M Previously Class, Architecture, Topology and Homologous superfamily - PDB-Sum server
FSSP
6U2MFold classification based on Structure-Structure alignment of Proteins - FSSP server
